Cas no 2110253-66-0 (ethyl 4-chloro-1,2-oxazole-3-carboxylate)
Ethyl 4-chloro-1,2-oxazole-3-carboxylate is a versatile heterocyclic compound featuring a chloro-substituted oxazole ring esterified at the 3-position. This structure imparts reactivity suitable for further functionalization, making it valuable in pharmaceutical and agrochemical synthesis. The chloro group enhances electrophilic substitution potential, while the ester moiety allows for hydrolysis or transesterification, enabling diverse derivatization pathways. Its stability under standard conditions ensures ease of handling in organic reactions. The compound serves as a key intermediate in the preparation of biologically active molecules, particularly in the development of antimicrobial and anti-inflammatory agents. Its well-defined reactivity profile and compatibility with common synthetic methodologies make it a practical choice for research and industrial applications.
2110253-66-0 structure
Product Name:ethyl 4-chloro-1,2-oxazole-3-carboxylate
CAS No:2110253-66-0
MF:C6H6ClNO3
MW:175.569740772247
CID:5413127
PubChem ID:165946695
Update Time:2025-06-08
ethyl 4-chloro-1,2-oxazole-3-carboxylate Chemical and Physical Properties
Names and Identifiers
-
- EN300-1653622
- ethyl 4-chloro-1,2-oxazole-3-carboxylate
- 2110253-66-0
- Z2732532172
- Ethyl 4-chloroisoxazole-3-carboxylate
-
- Inchi: 1S/C6H6ClNO3/c1-2-10-6(9)5-4(7)3-11-8-5/h3H,2H2,1H3
- InChI Key: UDNVJJWBXGYBND-UHFFFAOYSA-N
- SMILES: O1C=C(Cl)C(C(OCC)=O)=N1
Computed Properties
- Exact Mass: 175.0036207g/mol
- Monoisotopic Mass: 175.0036207g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 11
- Rotatable Bond Count: 3
- Complexity: 153
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 1.5
- Topological Polar Surface Area: 52.3?2
ethyl 4-chloro-1,2-oxazole-3-carboxylate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Enamine | EN300-1653622-0.05g |
ethyl 4-chloro-1,2-oxazole-3-carboxylate |
2110253-66-0 | 95% | 0.05g |
$315.0 | 2023-04-26 | |
| Enamine | EN300-1653622-0.1g |
ethyl 4-chloro-1,2-oxazole-3-carboxylate |
2110253-66-0 | 95% | 0.1g |
$470.0 | 2023-04-26 | |
| Enamine | EN300-1653622-0.25g |
ethyl 4-chloro-1,2-oxazole-3-carboxylate |
2110253-66-0 | 95% | 0.25g |
$672.0 | 2023-04-26 | |
| Enamine | EN300-1653622-0.5g |
ethyl 4-chloro-1,2-oxazole-3-carboxylate |
2110253-66-0 | 95% | 0.5g |
$1058.0 | 2023-04-26 | |
| Enamine | EN300-1653622-1.0g |
ethyl 4-chloro-1,2-oxazole-3-carboxylate |
2110253-66-0 | 95% | 1g |
$1357.0 | 2023-04-26 | |
| Enamine | EN300-1653622-2.5g |
ethyl 4-chloro-1,2-oxazole-3-carboxylate |
2110253-66-0 | 95% | 2.5g |
$2660.0 | 2023-04-26 | |
| Enamine | EN300-1653622-5.0g |
ethyl 4-chloro-1,2-oxazole-3-carboxylate |
2110253-66-0 | 95% | 5g |
$3935.0 | 2023-04-26 | |
| Enamine | EN300-1653622-10.0g |
ethyl 4-chloro-1,2-oxazole-3-carboxylate |
2110253-66-0 | 95% | 10g |
$5837.0 | 2023-04-26 | |
| Enamine | EN300-1653622-50mg |
ethyl 4-chloro-1,2-oxazole-3-carboxylate |
2110253-66-0 | 95.0% | 50mg |
$315.0 | 2023-09-21 | |
| Enamine | EN300-1653622-100mg |
ethyl 4-chloro-1,2-oxazole-3-carboxylate |
2110253-66-0 | 95.0% | 100mg |
$470.0 | 2023-09-21 |
ethyl 4-chloro-1,2-oxazole-3-carboxylate Related Literature
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Bin Han,Yasuo Shimizu,Gabriele Seguini,Celia Castro,Gérard Ben Assayag,Koji Inoue,Yasuyoshi Nagai,Sylvie Schamm-Chardon,Michele Perego RSC Adv., 2016,6, 3617-3622
-
Long Deng,Qian Zou,Biao Liu,Wenhui Ye,Chengfei Zhuo,Li Chen,Ze-Yuan Deng,Ya-Wei Fan,Jing Li Food Funct., 2018,9, 4234-4245
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Manickam Bakthadoss,Tadiparthi Thirupathi Reddy,Vishal Agarwal,Duddu S. Sharada Chem. Commun., 2022,58, 1406-1409
-
Peiyuan Zeng,Xiaoxiao Wang,Ming Ye,Qiuyang Ma,Jianwen Li,Wanwan Wang,Baoyou Geng,Zhen Fang RSC Adv., 2016,6, 23074-23084
-
Jonas Kind,Lukas Kaltschnee,Martin Leyendecker,Christina M. Thiele Chem. Commun., 2016,52, 12506-12509
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